Phenylmethyl 4-{4-[6-amino-2-{[(1S)-1-methylbutyl]oxy}-8-(methyloxy)-9H-purin-9-yl]butyl}-1-piperidinecarboxylate → 2-{[(1S)-1-Methylbutyl]oxy}-8-(methyloxy)-9-[4-(4-piperidinyl)butyl]-9H-purin-6-amine

HRID 1044924Notes

Reaction equation

HRID 1044924 reaction equation
C(OC1N=C2C(N=C(OC)N2CCCC2CCCCN2)=C(N)N=1)CCC.[NH2:27][C:28]1[N:36]=[C:35]([O:37][C@@H:38]([CH3:42])[CH2:39][CH2:40][CH3:41])[N:34]=[C:33]2[C:29]=1[N:30]=[C:31]([O:63][CH3:64])[N:32]2[CH2:43][CH2:44][CH2:45][CH2:46][CH:47]1[CH2:52][CH2:51][N:50](C(OCC2C=CC=CC=2)=O)[CH2:49][CH2:48]1>>[CH3:42][C@H:38]([O:37][C:35]1[N:34]=[C:33]2[C:29]([N:30]=[C:31]([O:63][CH3:64])[N:32]2[CH2:43][CH2:44][CH2:45][CH2:46][CH:47]2[CH2:48][CH2:49][NH:50][CH2:51][CH2:52]2)=[C:28]([NH2:27])[N:36]=1)[CH2:39][CH2:40][CH3:41]

Participants

3

Procedure

Prepared similarly to Intermediate 32 from phenylmethyl 4-{4-[6-amino-2-{[(1S)-1-methylbutyl]oxy}-8-(methyloxy)-9H-purin-9-yl]butyl}-1-piperidinecarboxylate.

Sources & evidence

ORD record
ord-4157421894944032abaa8025618626df
Source dataset
uspto-grants-2013_10
Patent number
US08563717B2

Reaction notes

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